Inspection Record

Hansamed Limited — Health Canada Inspection Findings

Health CanadaInspected 2021-07-06 13 findingsOther quality systemStability and storageEquipment and facilityComplaint and recall handlingRegulatory reporting and change controlDeviation, CAPA, and investigationLabeling and packaging

View the regulator's official source The source document is always the basis for judgement.

Findings

1Other quality system

The controls were inadequate for creating, modifying, reviewing, storing, and/or retrieving records.

2Stability and storage

The temperature and/or humidity control was inadequate.

3Equipment and facility

The maintenance of records was inadequate.

4Other quality system

The implementation of a self-inspection program was inadequate.

5Complaint and recall handling

The written procedures for recalls were inadequate.

6Regulatory reporting and change control

The change control system was inadequate for ensuring changes are properly documented, evaluated, and/or approved.

7Equipment and facility

The premises were not designed, constructed, and/or maintained to prevent the entry of pests and/or foreign material into the building.

8Deviation, CAPA, and investigation

Investigations into deviations, reports, and/or follow-up actions were inadequate.

9Equipment and facility

The availability, content and/or maintenance of the quality agreements between the supplier, fabricator, tester, packager, labeller, distributor, importer, and/or wholesaler was inadequate.

10Complaint and recall handling

The quality control department's handling of complaints and/or information received about drug quality was inadequate.

11Other quality system

Tests were not performed according to approved specifications.

12Labeling and packaging

The importer did not ensure that the foreign sites use to fabricate, package/label, or test drug products met the requirements described in Guidance on Evidence to Demonstrate Drug GMP Compliance of Foreign Sites (GUI-0080).

13Other quality system

The assessment to release finished products was inadequate.

About this record

Extracted automatically from the document of the Health Canada inspection on 2021-07-06. The source is available at the link above.

This is a record of that moment. Inspection findings are usually followed by the company's response and corrective action, but this page does not know how that turned out. Do not read it as the current state; check the regulator's official announcements for the latest status.

Translation and classification are automated and may differ in nuance from the source.

Other records for this company

Hansamed Limited findings history — including this company's other documents Health Canada documents, 2021 Go to Findings search